Yuviwel Patent Expiration

Yuviwel is a drug owned by Ascendis Pharma Growth Disorders As. It is protected by 12 US drug patents filed in 2026 out of which none have expired yet. Based on its patents and exclusivities, its generic launch date is estimated to be Nov 12, 2042. Details of Yuviwel's patents and their expiration are given in the table below.

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Drug Patent Number Drug Patent Title Drug Patent Expiry Status
These drug patents protect the active ingredient(API) of the drug. Only drug patent owner can launch products that use this active ingredient until these patents expire.
US10835578 Cnp Prodrugs With Large Carrier Moieties
Jan, 2037

(10 years from now)

Active
US11413351 Cnp Prodrugs With Carrier Attachment At The Ring Moiety
Jan, 2037

(10 years from now)

Active
US11154593 Cnp Prodrugs With Large Carrier Moieties
Jan, 2037

(10 years from now)

Active
US11311604 Controlled-Release Cnp Agonists With Low Npr-C Binding
Jan, 2037

(10 years from now)

Active
US11389510 Controlled-Release Cnp Agonists With Low Initial Npr-B Activity
Jan, 2037

(10 years from now)

Active
US11224661 Controlled-Release Cnp Agonists With Increased Nep Stability
Jan, 2037

(10 years from now)

Active
US8906847 Prodrug comprising a drug linker conjugate
Apr, 2031

(5 years from now)

Active
These drug patents focus on the other aspects of the drug like dosage, mode of administration (oral, tablet, capsules, liquids etc).
US12377133 Dry Pharmaceutical Formulations Of Cnp Conjugates
Nov, 2042

(16 years from now)

Active
US12239689 Controlled-Release Cnp Agonists With Low Initial Npr-B Activity
Jan, 2037

(10 years from now)

Active
US12083182 Controlled-Release Cnp Agonists With Increased Nep Stability
Jan, 2037

(10 years from now)

Active
US11389511 Controlled-Release Cnp Agonists With Reduced Side-Effects
Jan, 2037

(10 years from now)

Active
US12156917 Cnp Prodrugs With Carrier Attachment At The Ring Moiety
Jan, 2037

(10 years from now)

Active


FDA has granted several exclusivities to Yuviwel. Till the time these exclusivities are active, no other company can market a generic or bioequivalent version of Yuviwel, regardless of the status of it's patents. These exclusivities hence play a crucial role in delaying the generic launch. Given below are details of the exclusivities granted to Yuviwel.

Exclusivity Information

Yuviwel holds 1 exclusivities out of which none have expired. Its last outstanding exclusivity is set to expire in 2033. Details of Yuviwel's exclusivity codes and their expiration dates are given below.


Drug Exclusivity Drug Exclusivity Expiration
Orphan Drug Exclusivity(ODE-516) Feb 27, 2033

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US patents provide insights into the exclusivity only within the United States, but Yuviwel is protected by patents in multiple countries. Understanding the full scope of patent protection is crucial in strategizing market entry. By looking at the broader patent landscape, you can identify markets with weaker patent protection which could be ideal generic entry points. The following section offers details on Yuviwel's family patents as well as insights into ongoing legal events on those patents.

Yuviwel's Family Patents


Family Patents

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Generic Launch

Generic Release Date:

Yuviwel's generic launch date based on the last expiry date of its patents and exclusivities combined is estimated to be Nov 12, 2042 (This date is subject to change depending upon the patent filing activities by the drug owner or exclusivity additions to its drug application)

Yuviwel Generics:

There are no approved generic versions for Yuviwel as of now.





About Yuviwel

Yuviwel is a drug owned by Ascendis Pharma Growth Disorders As. Yuviwel uses Navepegritide as an active ingredient. Yuviwel was launched by Ascendis in 2026.

Approval Date:

Yuviwel was approved by FDA for market use on 27 February, 2026.

Active Ingredient:

Yuviwel uses Navepegritide as the active ingredient. Check out other Drugs and Companies using Navepegritide ingredient

Dosage:

Yuviwel is available in powder form for subcutaneous use. Given below is detailed information on Dosage -

Strength Dosage Form Availability Application Pathway
1.3MG/VIAL POWDER Prescription SUBCUTANEOUS
2.8MG/VIAL POWDER Prescription SUBCUTANEOUS
5.5MG/VIAL POWDER Prescription SUBCUTANEOUS